Variant (rsID / SNP)

rs41277763

rs41277763 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCA1. Location: chromosome 9, position 107,566,930. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ABCA1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 9:107566930
Cytoband: 9q31.1
HGVS: NM_005502.4(ABCA1):c.4536G>T (p.Thr1512=)
Allele change: Synonymous_T1512T

Associated conditions / phenotypes

Tangier disease|Hypoalphalipoproteinemia, primary, 1

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.